A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609716



Internal ID20982787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40251762..40319261hg38UCSC Ensembl
chr7:40291361..40358860hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3867500
hg1967500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153760
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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